Department of Neurosurgery, Chonnam National University Hwasun Hospital, 160, Ilsim-ri, Hwasun-eup, Hwasun-gun, Jeollanam-do 519-809, Republic of Korea.
J Neurooncol. 2011 May;103(1):103-10. doi: 10.1007/s11060-010-0353-z. Epub 2010 Aug 25.
Oligodendroglial tumors sometimes show heterogeneous ring enhancement with a central necrotic portion. We aimed to reveal the prognosis of such tumors based on such radiologic findings and compare them to other prognostic factors. Participants were 32 patients with oligodendroglioma (17 oligodendrogliomas, 15 anaplastic oligodendrogliomas) who underwent surgery from 2004 to 2008. We investigated tumor radiologic findings, locations, calcification, whether localized or diffuse type, and enhancement patterns. Of other prognostic factors, we analyzed age, sex, pathology, extent of removal, adjuvant therapy, genetic change in 1p and 19q, and MGMT methylation status. We checked for genetic abnormality in 1p and 19q using the FISH method. To investigate MGMT methylation, we performed methylation-specific PCR (MSP). Mean follow-up duration was 3.2 years. Median age was 42.4 years, and the male:female ratio was 21:11. Out of 17 oligodendrogliomas, 14 (82.4%) showed combined 1p/19q deletion, and 14 (82.4%), methylated MGMT. Among 15 anaplastic oligodendrogliomas, there were 7 (46.6%) with combined 1p/19q deletion and 11 (73.3%) with methylated MGMT. The 4-year recurrence-free survival and overall survival were 77.6 and 100% in oligodendrogliomas and 59.1 and 71.6% in anaplastic oligodendrogliomas, respectively. On univariate analysis, radiologic variable of ring enhancement pattern was statistically significant related with recurrence-free survival (P = 0.003). Variables such as sex (P = 0.03), combined 1p/19q loss (P = 0.04), tumor location (P = 0.02), and anaplastic pathology (P = 0.04) were significantly correlated with overall survival. Cox's regression model revealed that ring enhancement pattern was associated with frequent recurrence (ring enhancement, hazard ratio = 8.281, P = 0.04), and these showed 1p deletion only. Anaplastic oligodendrogliomas with ring enhancement like glioblastomas and without combined 1p/19q loss should receive close follow-up after treatment because of frequent recurrences.
少突胶质细胞瘤有时表现为伴有中央坏死部分的不均匀环状增强。我们旨在根据这些影像学发现揭示此类肿瘤的预后,并将其与其他预后因素进行比较。参与者为 2004 年至 2008 年间接受手术的 32 名少突胶质细胞瘤患者(17 名少突胶质细胞瘤患者,15 名间变性少突胶质细胞瘤患者)。我们研究了肿瘤的影像学发现、位置、钙化、局限性或弥漫性类型以及增强模式。在其他预后因素方面,我们分析了年龄、性别、病理学、切除程度、辅助治疗、1p 和 19q 的遗传改变以及 MGMT 甲基化状态。我们使用 FISH 方法检查了 1p 和 19q 的遗传异常。为了研究 MGMT 甲基化,我们进行了甲基化特异性 PCR(MSP)。平均随访时间为 3.2 年。中位年龄为 42.4 岁,男女比例为 21:11。17 名少突胶质细胞瘤中有 14 名(82.4%)显示 1p/19q 联合缺失,14 名(82.4%)MGMT 甲基化。在 15 名间变性少突胶质细胞瘤中,有 7 名(46.6%)联合 1p/19q 缺失,11 名(73.3%)MGMT 甲基化。少突胶质细胞瘤的 4 年无复发生存率和总生存率分别为 77.6%和 100%,间变性少突胶质细胞瘤分别为 59.1%和 71.6%。单因素分析显示,环状增强模式的影像学变量与无复发生存率有统计学意义(P=0.003)。性别(P=0.03)、联合 1p/19q 缺失(P=0.04)、肿瘤位置(P=0.02)和间变性病理学(P=0.04)等变量与总生存率显著相关。Cox 回归模型显示,环状增强模式与频繁复发相关(环状增强,风险比=8.281,P=0.04),且仅存在 1p 缺失。具有环状增强的间变性少突胶质细胞瘤,类似于胶质母细胞瘤且不伴有联合 1p/19q 缺失,治疗后应密切随访,因为其复发频繁。